Issue 30, 2022

One-step high-yield preparation of nitrogen- and sulfur-codoped carbon dots with applications in chromium(vi) and ascorbic acid detection

Abstract

In this research, a nitrogen- (N) and sulfur- (S) codoped carbon dot (CDs-IPM)-based sensor was synthesized using a single-step hydrothermal method. Specifically, microcrystalline cellulose (MCC) was the main raw material, which was extracted from banana pseudo-stem-based waste, while autonomous sulfonic acid-functionalized ionic liquid (SO3H-IL) and polyethylene glycol 400 (PEG 400) acted as the N, S dopant, and surface modifier, respectively. Comprehensive spectroscopic characterization of the synthesized CDs-IPM revealed the introduction of S, N atoms in the matrix with existence of surface oxygenic functional groups. The CDs-IPM possessed enhanced photoluminescence (PL) intensity, synthetic yield, and PL quantum yield (PLQY). Additionally, electron transfer between the CDs-IPM, hexavalent chromium (Cr(VI)), and subsequent ascorbic acid (AA) succeeded in turning the fluorescence on and off. The detection limit was 17 nM for Cr(VI), while it was 103 nM for AA. Our study data can simplify the process of synthesis of CDs utilizing biodegradable starting materials. The probe reported in this study may serve as a valuable addition to the field of environment monitoring by virtue of its enhanced detection sensitivity, high selectivity, and stability.

Graphical abstract: One-step high-yield preparation of nitrogen- and sulfur-codoped carbon dots with applications in chromium(vi) and ascorbic acid detection

Supplementary files

Article information

Article type
Paper
Submitted
18 Mar 2022
Accepted
26 May 2022
First published
13 Jul 2022
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2022,12, 19686-19694

One-step high-yield preparation of nitrogen- and sulfur-codoped carbon dots with applications in chromium(VI) and ascorbic acid detection

F. Meng, H. Xu, S. Wang, J. Wei, W. Zhou, Q. Wang, P. Li, F. Kong and Y. Zhang, RSC Adv., 2022, 12, 19686 DOI: 10.1039/D2RA01758J

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